Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D02YEE
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| Former ID |
DNC010180
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| Drug Name |
N-benzyl-6-(3,3,3-trifluoropropoxy)nicotinamide
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| Synonyms |
CHEMBL576449; N-benzyl-6-(3,3,3-trifluoropropoxy)nicotinamide
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
| Structure |
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Download2D MOL |
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| Formula |
C16H15F3N2O2
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| Canonical SMILES |
C1=CC=C(C=C1)CNC(=O)C2=CN=C(C=C2)OCCC(F)(F)F
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| InChI |
1S/C16H15F3N2O2/c17-16(18,19)8-9-23-14-7-6-13(11-20-14)15(22)21-10-12-4-2-1-3-5-12/h1-7,11H,8-10H2,(H,21,22)
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| InChIKey |
KOPBISOWPWQPSS-UHFFFAOYSA-N
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Soluble epoxide hydrolase (EPHX2) | Target Info | Inhibitor | [1] |
| KEGG Pathway | Arachidonic acid metabolism | |||
| Metabolic pathways | ||||
| Peroxisome | ||||
| Pathwhiz Pathway | Arachidonic Acid Metabolism | |||
| WikiPathways | Metapathway biotransformation | |||
| Arachidonate Epoxygenase / Epoxide Hydrolase | ||||
| Arachidonic acid metabolism | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Design and synthesis of substituted nicotinamides as inhibitors of soluble epoxide hydrolase. Bioorg Med Chem Lett. 2009 Oct 15;19(20):5864-8. | |||
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